Canonical Allele Identifier: CA340526180
Gene: TACSTD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.58576751T>G , CM000663.2:g.58576751T>G GRCh38
NC_000001.10:g.59042423T>G , CM000663.1:g.59042423T>G GRCh37
NC_000001.9:g.58815011T>G NCBI36
NG_016237.1:g.5744A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371225.4:c.406A>C MANE Select ENSP00000360269.2:p.Thr136Pro
ENST00000371225.3:c.406A>C ENSP00000360269.2:p.Thr136Pro
NM_002353.2:c.406A>C NP_002344.2:p.Thr136Pro
NM_002353.3:c.406A>C MANE Select NP_002344.2:p.Thr136Pro